• Senior Director of Value & Access Strategy (V&A)

    Teva Pharmaceuticals (Parsippany, NJ)
    …SP, LTC, 340B, etc.), copay This role is responsible for brands across the product life cycle: pre- product launch, launch, in-line, and mature. This role manages ... the access landscape, develop and execute research, develop strategies to achieve product access goals across all key stakeholders listed above. In addition, this… more
    Teva Pharmaceuticals (08/17/25)
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  • Sr Commercial Quality Manager NA

    Reckitt (Parsippany, NJ)
    …units, distribution centers, and embellishers. This includes assuring that all product specifications and all regulatory requirements have been satisfied prior to ... the final release of any product into the distribution channel. + Provide leadership to...+ Coordination of resolution of any quality, compliance and safety issues affecting products in market + In conjunction… more
    Reckitt (08/08/25)
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  • Director, AI/ML Platform Engineering Lead

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …our next-generation platforms for Generative AI, LLMOps, and MLOps within a pharmaceutical environment. This role is pivotal in enabling the responsible and ... by cross-functional teams. + Collaborate with business partners, data scientists, and product owners to identify, prioritize, and deliver high-value AI use cases. +… more
    Otsuka America Pharmaceutical Inc. (07/23/25)
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  • Manager NA GS Supply Chain

    J&J Family of Companies (New Brunswick, NJ)
    …for humanity. Learn more at https://www.jnj.com **Job Function:** Environmental Health, Safety (EH&S) and Facilities Services (FS) **Job Sub** **Function:** Physical ... The focus of this work is on protecting patient safety and securing the supply chain against illicit actions,... and securing the supply chain against illicit actions, product theft, missing or lost shipments, terrorism, and unauthorized… more
    J&J Family of Companies (08/16/25)
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  • VP Clinical Development, Oncology

    Sumitomo Pharma (Trenton, NJ)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... teams from preclinical experiments to the end of the product 's life cycle. + Clinical Trial Oversight: Develop and...protocols. + Oversee clinical trial execution, ensuring quality, patient safety , and compliance with GCP standards. + Develop and… more
    Sumitomo Pharma (08/14/25)
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  • Sr Specialist, External Quality Small Molecules

    Kelly Services (Titusville, NJ)
    …consistent delivery of pharmaceutical products that meet or exceed safety , regulatory compliance, and product standards. **Key Responsibilities:** + Provide ... and approve quality systems documentation, including batch documentation and annual product reviews. + Assess change controls and execute activities for implementing… more
    Kelly Services (08/14/25)
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  • Director US Labeling & Registration

    Bayer (NJ)
    …and local RA staff. The position also contributes to the development of US product launch planning strategies and interacts with product life cycle teams to ... precedents and opportunities for FDA interactions; + Partners with Product Supply Labeling Development/artwork staff; + Demonstrates, credibly embodies and… more
    Bayer (08/07/25)
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  • Field Inventory Specialist

    Terumo Medical Corporation (Somerset, NJ)
    …and third-party warehousing, general accounting projects. + Demonstrate a commitment to patient safety and product quality by maintaining compliance with all TMC ... of agreements as well as compliance with policies and procedures. Will analyze product turnover to determine optimal stock rotation to reduce losses from expiry and… more
    Terumo Medical Corporation (07/09/25)
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  • Manufacturing Operator 2nd shift (Compression)

    System One (Cranbury, NJ)
    …ideal candidate is mechanically inclined, detail-oriented, and committed to consistent product quality and safety . Responsibilities Production Operations + ... the production of solid oral dosage forms in a cGMP-regulated pharmaceutical environment. This role involves equipment setup, in-process testing, documentation, and… more
    System One (08/03/25)
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  • Senior Manager - Patient Access Programs Program…

    Novo Nordisk (Plainsboro, NJ)
    …Public Affairs, Public Policy, Managed Markets, Regulatory, Legal, IT, Trade, Product Safety and Compliance. External relationships include affordability program ... with us? The Position Responsible for overseeing and managing all NNI patient product access programs to ensure Novo Nordisk's commitment to patient-centered care as… more
    Novo Nordisk (08/13/25)
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